K-number	K083510
Device name	KUBTEC XPERT 20
Applicant	Kub Technologies, Inc.
Product code	KPR
Device class	Class II
Decision date	Jan 8, 2009
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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KUBTEC XPERT 20

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